Overview
Our laboratory is
interested in understanding underlying mechanisms of ocular angiogenesis
and the abnormalities in this process that lead to retinal vascular disease.
Since abnormal angiogenesis is frequently the final common pathway leading
to the vast majority of diseases that result in catastrophic loss of vision,
we are also interested in understanding mechanisms of retinal degeneration
that lead to ocular angiogenesis. This aspect of our program focuses on
the role of polytopic membrane proteins of visual importance that are
mutated in certain inherited retinal degenerations. While most of our
effort is devoted to understanding ocular angiogenesis, the role of abnormal
membrane protein targeting and integration provides an alternate approach
to identifying potential therapeutic avenues to treating diseases for
which there are currently no effective treatments. Finally, a third component
of our research program focuses on developing physiologically relevant
animal models of ocular angiogenesis and drug delivery systems useful
in the treatment of human retinal neovascular and degenerative diseases.
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